ONKI3 | Medical Subject Headings

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Hermanski-Pudlak Syndrome

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ Hermanski-Pudlak Syndrome 17 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Eye Diseases, Hereditary ∟ Albinism ∟ Albinism, Oculocutaneous ∟ Hermanski-Pudlak Syndrome 17 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Amino Acid Metabolism, Inborn Errors ∟ Albinism ∟ Albinism, Oculocutaneous ∟ Hermanski-Pudlak Syndrome 17 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Albinism ∟ Albinism, Oculocutaneous ∟ Hermanski-Pudlak Syndrome 17 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Diseases, Hereditary ∟ Albinism ∟ Albinism, Oculocutaneous ∟ Hermanski-Pudlak Syndrome 17 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ Hermanski-Pudlak Syndrome 17 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Platelet Storage Pool Deficiency ∟ Hermanski-Pudlak Syndrome 17 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Platelet Disorders ∟ Platelet Storage Pool Deficiency ∟ Hermanski-Pudlak Syndrome 17 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemorrhagic Disorders ∟ Platelet Storage Pool Deficiency ∟ Hermanski-Pudlak Syndrome 17 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Amino Acid Metabolism, Inborn Errors ∟ Albinism ∟ Albinism, Oculocutaneous ∟ Hermanski-Pudlak Syndrome 17 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Pigmentation Disorders ∟ Hypopigmentation ∟ Albinism ∟ Albinism, Oculocutaneous ∟ Hermanski-Pudlak Syndrome 17 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Albinism ∟ Albinism, Oculocutaneous ∟ Hermanski-Pudlak Syndrome 17 coordinate concepts ∟ Activated Protein C Resistance \| ∟ Afibrinogenemia \| ∟ Antithrombin III Deficiency \| ∟ Bernard-Soulier Syndrome \| ∟ Factor V Deficiency \| ∟ Factor VII Deficiency \| ∟ Factor X Deficiency \| ∟ Factor XI Deficiency \| ∟ Factor XII Deficiency \| ∟ Factor XIII Deficiency \| ∟ Hemophilia A \| ∟ Hemophilia B \| ∟ Hypoprothrombinemias \| ∟ Protein C Deficiency \| ∟ Thrombasthenia \| ∟ von Willebrand Disease \| ∟ Wiskott-Aldrich Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Blood Coagulation Disorders, Inherited ∟ Hermanski-Pudlak Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Eye Diseases, Hereditary ∟ Albinism ∟ Albinism, Oculocutaneous ∟ Hermanski-Pudlak Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Metabolism, Inborn Errors ∟ Amino Acid Metabolism, Inborn Errors ∟ Albinism ∟ Albinism, Oculocutaneous ∟ Hermanski-Pudlak Syndrome Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Skin Diseases, Genetic ∟ Albinism ∟ Albinism, Oculocutaneous ∟ Hermanski-Pudlak Syndrome Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Diseases, Hereditary ∟ Albinism ∟ Albinism, Oculocutaneous ∟ Hermanski-Pudlak Syndrome Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Blood Coagulation Disorders, Inherited ∟ Hermanski-Pudlak Syndrome Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Coagulation Disorders ∟ Platelet Storage Pool Deficiency ∟ Hermanski-Pudlak Syndrome Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Blood Platelet Disorders ∟ Platelet Storage Pool Deficiency ∟ Hermanski-Pudlak Syndrome Medical Subject Headings (MeSH) ∟ Hemic and Lymphatic Diseases ∟ Hematologic Diseases ∟ Hemorrhagic Disorders ∟ Platelet Storage Pool Deficiency ∟ Hermanski-Pudlak Syndrome Medical Subject Headings (MeSH) ∟ Nutritional and Metabolic Diseases ∟ Metabolic Diseases ∟ Metabolism, Inborn Errors ∟ Amino Acid Metabolism, Inborn Errors ∟ Albinism ∟ Albinism, Oculocutaneous ∟ Hermanski-Pudlak Syndrome Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Pigmentation Disorders ∟ Hypopigmentation ∟ Albinism ∟ Albinism, Oculocutaneous ∟ Hermanski-Pudlak Syndrome Medical Subject Headings (MeSH) ∟ Skin and Connective Tissue Diseases ∟ Skin Diseases ∟ Skin Diseases, Genetic ∟ Albinism ∟ Albinism, Oculocutaneous ∟ Hermanski-Pudlak Syndrome Blood Coagulation Disorders, Inherited > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Albinism, Oculocutaneous > Albinism > Eye Diseases, Hereditary > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Albinism, Oculocutaneous > Albinism > Amino Acid Metabolism, Inborn Errors > Metabolism, Inborn Errors > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Albinism, Oculocutaneous > Albinism > Skin Diseases, Genetic > Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Albinism, Oculocutaneous > Albinism > Eye Diseases, Hereditary > Eye Diseases > Medical Subject Headings (MeSH) Blood Coagulation Disorders, Inherited > Blood Coagulation Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Platelet Storage Pool Deficiency > Blood Coagulation Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Platelet Storage Pool Deficiency > Blood Platelet Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Platelet Storage Pool Deficiency > Hemorrhagic Disorders > Hematologic Diseases > Hemic and Lymphatic Diseases > Medical Subject Headings (MeSH) Albinism, Oculocutaneous > Albinism > Amino Acid Metabolism, Inborn Errors > Metabolism, Inborn Errors > Metabolic Diseases > Nutritional and Metabolic Diseases > Medical Subject Headings (MeSH) Albinism, Oculocutaneous > Albinism > Hypopigmentation > Pigmentation Disorders > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) Albinism, Oculocutaneous > Albinism > Skin Diseases, Genetic > Skin Diseases > Skin and Connective Tissue Diseases > Medical Subject Headings (MeSH) X
History note:	Albinism, Oculocutaneous (1990-2000)X
historyNote*:	2001 X
publicMeSHNote*:	2001 X
Scope note:	Syndrome characterized by the triad of oculocutaneous albinism (ALBINISM, OCULOCUTANEOUS); PLATELET STORAGE POOL DEFICIENCY; and lysosomal accumulation of ceroid lipofuscin. X
activeMeSHYear*:	2007X
dateCreated*:	2000-06-22X
dateEstablished*:	2001-01-01X
dateRevised*:	2006-07-05X
recordAuthorizer*:	sjnX
recordMaintainer*:	lktX
recordOriginator*:	agsX
Type:	Concept X
Coordinate terms:	Activated Protein C Resistance \| Afibrinogenemia \| Antithrombin III Deficiency \| Bernard-Soulier Syndrome \| Factor V Deficiency \| Factor VII Deficiency \| Factor X Deficiency \| Factor XI Deficiency \| Factor XII Deficiency \| Factor XIII Deficiency \| Hemophilia A \| Hemophilia B \| Hypoprothrombinemias \| Protein C Deficiency \| Thrombasthenia \| von Willebrand Disease \| Wiskott-Aldrich Syndrome X
URI:	X
Labels and equivalent concepts:	Hermanski-Pudlakin oireyhtymä (fi) Hermanski-Pudlakin syndrooma (fi, replaced) Hermanski-Pudlaks syndrom (sv) Hermansky-Pudlak Syndrome (en, replaced) Syndroma Hermanski-Pudlak (la-FI, replaced) X
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